FDA 510(k) Applications Submitted by RICHARD TYSON
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K031942 | 06/24/2003 | XPECT GIARDIA LATERAL FLOW ASSAY, MODEL 2450020 | REMEL INC |
| K031965 | 06/26/2003 | XPECT CRYPTOSPORIDIUM LATERAL FLOW ASSAY, MODEL 2451020 | REMEL INC |
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